Schirrmacher V, Cheingsong-Popov R, Arnheiter H
J Exp Med. 1980 Apr 1;151(4):984-9. doi: 10.1084/jem.151.4.984.
Murine hepatocytes, isolated by an in situ collagenase-perfusion technique and cultured in Petri dishes, were shown to form rosettes with liver-metastasizing syngeneic tumor cells. Pretreatment of the tumor cells with neuraminidase generally increased the binding, whereas pretreatment of the liver cells with neuraminidase abolished the binding completely. The tumor-cell binding may be mediated by the previously described lectin-like receptor of hepatocytes that also was sensitive to neuraminidase treatment and that bound desialylated cells better than normal cells. Anti-H-2 sera could efficiently inhibit the rosette formation of metastatic tumor cells with the hepatocytes, which points to a possible role of H-2 molecules in this interaction of neoplastic and normal cells.
通过原位胶原酶灌注技术分离并培养在培养皿中的小鼠肝细胞,被证明能与肝脏转移性同基因肿瘤细胞形成玫瑰花结。用神经氨酸酶预处理肿瘤细胞通常会增加结合,而用神经氨酸酶预处理肝细胞则会完全消除结合。肿瘤细胞的结合可能是由先前描述的肝细胞凝集素样受体介导的,该受体对神经氨酸酶处理也敏感,并且与去唾液酸化细胞的结合优于正常细胞。抗H-2血清可以有效抑制转移性肿瘤细胞与肝细胞的玫瑰花结形成,这表明H-2分子在肿瘤细胞与正常细胞的这种相互作用中可能发挥作用。